Clarissa Elysia Fu
The prognostic value of including non‐alcoholic fatty liver disease in the definition of metabolic syndrome
Fu, Clarissa Elysia; Yong, Jie Ning; Ng, Cheng Han; Nah, Benjamin; Chew, Nicholas W. S.; Chin, Yip Han; Kong, Gwyneth; Tan, Darren Jun Hao; Lim, Wen Hui; Lim, Lincoln Kai En; Zeng, Rebecca Wenling; Shabbir, Asim; Tan, Eunice X. X.; Huang, Daniel Q.; Khoo, Chin Meng; Siddqui, Mohammad Shadab; Chan, Mark Y. Y.; Noureddin, Mazen; Mamas, Mamas A.; Muthiah, Mark
Authors
Jie Ning Yong
Cheng Han Ng
Benjamin Nah
Nicholas W. S. Chew
Yip Han Chin
Gwyneth Kong
Darren Jun Hao Tan
Wen Hui Lim
Lincoln Kai En Lim
Rebecca Wenling Zeng
Asim Shabbir
Eunice X. X. Tan
Daniel Q. Huang
Chin Meng Khoo
Mohammad Shadab Siddqui
Mark Y. Y. Chan
Mazen Noureddin
Mamas Mamas m.mamas@keele.ac.uk
Mark Muthiah
Abstract
Background/Aims Metabolic syndrome (MetS) affects over one third of the US adult population. Despite its close association with non-alcoholic fatty liver disease (NAFLD), the traditional definition of MetS does not account for the presence of NAFLD. The present study thus aims to evaluate the inclusion of NAFLD in the diagnostic criteria of metabolic syndrome on its accuracy of capturing individuals with metabolic dysregulation and its prediction of adverse events. Methods Data collected from NHANES between 1999 and 2018 was analysed. Clinical characteristics and outcomes between individuals with metabolic syndrome from both the American Heart Association/National Heart, Lung, and Blood Institute (MetS) and the study's proposed diagnostic criteria (MetS2) were evaluated. Outcomes in both groups were evaluated with multivariate analyses, and further subgroup analysis on individuals matched with Coarsened Exact Matching was performed. Results Of 46,184 individuals included, 32.54% and 40.54% fulfilled MetS and MetS2 criteria respectively. Considering NAFLD in the definition of metabolic syndrome, a further 8.00% (n = 3694) were included. MetS was significantly associated with all-cause (HR: 1.184, 95% CI: 1.110–1.263, p?<?0.001) and cardiovascular disease (CVD) mortality (SHR: 1.288, 95% CI: 1.233–1.347, p?<?0.001), and major adverse cardiovascular events (MACE). MetS2 was similarly associated with all-cause (HR: 1.175, 95% CI: 1.088–1.269, p?<?0.001), CVD mortality (SHR: 1.283, 95% CI: 1.245–1.323, p?<?0.001) and MACE. Conclusion Inclusion of NAFLD allows for identification a greater proportion of the population with metabolic risk. This allows for early intervention and potential to lift some burden off the global healthcare system.
Journal Article Type | Article |
---|---|
Acceptance Date | Jan 8, 2023 |
Online Publication Date | Jan 29, 2023 |
Publication Date | May 1, 2023 |
Journal | Alimentary Pharmacology & Therapeutics |
Print ISSN | 0269-2813 |
Publisher | Wiley |
Volume | 57 |
Issue | 9 |
Pages | 979-987 |
DOI | https://doi.org/10.1111/apt.17397 |
Keywords | Pharmacology (medical), Gastroenterology, Hepatology |
Publisher URL | https://onlinelibrary.wiley.com/doi/10.1111/apt.17397 |